Advia® 2120i Hematology System
The ADVIA 2120i is an automated haematology analyser for quantitative in vitro diagnostic testing in clinical laboratories. It provides complete blood counts, leukocyte differentials,…
The ADVIA 2120i is an automated haematology analyser for quantitative in vitro diagnostic testing in clinical laboratories. It provides complete blood counts, leukocyte differentials, reticulocyte analysis and nucleated red-cell counts, with additional body-fluid cell-count applications.
An analytical module aspirates, dilutes and analyses samples. The autosampler mixes and identifies specimens and presents them for processing. A computer workstation controls the instrument and manages the resulting data.
Specimen Scope
The stated specimen range includes whole blood and pleural, peritoneal and peritoneal-dialysis fluids with K2 or K3 EDTA, together with cerebrospinal fluid for the specified cell counts.
3manufacturers in China registered for this device type
3catalogue numbers in this listing
3510(k) clearances naming this product code
23recalls on this code
Who Else Makes It
Concentrated in Guangdong (2), Jiangsu (1). One is registered as a contract manufacturer, able to build to a specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| VTech Communications Ltd | Dongguan | Guangdong | Contract manufacturer | 5 |
| Shenzhen Mindray BIO-Medical Electronics Co., Ltd. | Shenzhen | Guangdong | Specification developer | 61 |
| Onechipdx Biotech (Suzhou) Co., Ltd. | Suzhou | Jiangsu | Specification developer | 2 |
Record
| Listed by | Siemens Healthcare Diagnostics Inc, United States |
|---|---|
| FDA product code | GKZ |
| Device type | Counter, Differential Cell |
| Device class | Class 2 |
| Regulation | 21 CFR 864.5220 |
| Establishment | Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K102644 |
| Record published | 2016-09-24 |
| Record revised | 2024-05-16 (version 8) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Label carries | serial number |
| Storage | Storage environment temperature 15 to 25 °C |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 10285573 | In distribution | |
| 10285572 | In distribution | |
| 10488923 | In distribution |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| QBC Diagnostics | Drucker Diagnostics, LLC | 41 |
| Cell-DYN | Abbott Laboratories | 19 |
| Research and Diagnostic Systems | Research AND Diagnostic Systems, Inc. | 17 |
| Simultest | Becton, Dickinson AND Company | 10 |
| BD FACSCanto™ | Becton, Dickinson AND Company | 10 |
| FACSCanto | Becton, Dickinson AND Company | 7 |
| BD Multitest | Becton, Dickinson AND Company | 6 |
| Coulter AcT | Beckman Coulter, Inc. | 6 |
| BD™ Multi-Check | Becton, Dickinson AND Company | 6 |
| BD Tritest | Becton, Dickinson AND Company | 6 |
| Coulter LH | Beckman Coulter, Inc. | 5 |
| HemoScreen | Pixcell Medical Inc. | 5 |
Showing 12 of 245. All products under Counter, Differential Cell
510(K) Clearances
| Clearance | Decision date |
|---|---|
| K162977 | 2017-08-11 |
| K102644 | 2011-11-23 |
| K090346 | 2010-07-28 |
Recalls Naming This Product
21 recalls name this product by its own identifiers, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | ||
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 32 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 1 unit | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 7 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 15 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 187 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 1 unit | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 1 unit | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 8 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 185 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 132 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 283 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 195 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 43 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 969 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 1452 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 33 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 27 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 572 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2021-03-05 | Class II | Under Investigation by firm | Potential Sample Identification (SID) Mismatch with14-Character Barcodes | 674 units | |
| Siemens Healthcare Diagnostics Inc | 510(k) number | 2013-08-12 | Class II | Software design | Siemens determined that if an autosampler rack jam error occurs during operation of an ADVIA 2120/2120i connected to an ADVIA Autoslide, it is possible that the next slide processed by the Autoslide could be labeled with the wrong sample id | 311 units total (US: 51 units; Foreign: 260 units) | 2015-11-18 |
Recalls
2 of these are Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.
| Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|
| 2016-10-21 | Class II | Software design | Siemens is investigating an issue which may cause an incorrect result to be reported. Siemens received two reports of multiple discordant records for the same Sample ID in the ADVIA 560 Hematology System database that occurred during the in | US: 23 systems; Foreign: 141 systems | 2018-06-07 |
| 2016-03-10 | Class II | Process design | Software anomaly; Siemens identified that software version 1.4.2133 on the ADVIA 560 Hematology System does not trigger the following flags: The G or L morphology flags for immature granulocytes (IG) and atypical lymphocytes (ATYP), respect | US: 8 systems; Foreign: 64 systems | 2018-06-07 |
Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.